FDA Device Establishments · JSON-LD · Markdown
FEI 3005813632 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3005813632 |
|---|---|
| Owner / Operator | BIEGLER GMBH (#9069662) |
| Address | ALLHANGSTRASSE 18A, MAUERBACH Niederosterreich, 3001, AT |
| Mandatory US Agent | ProMedic, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FMF |
| Regulation § (21 CFR) | 880.5860 |
| Proprietary names | Duplocath |
Source: openFDA. Public-domain (CC0).